A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778432



Internal ID19161628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:136725859..136806153hg38UCSC Ensembl
Innerchr9:139620311..139700605hg19UCSC Ensembl
Innerchr9:138740132..138820426hg18UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3880295
hg1980295
hg1880295
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3891732
Supporting Variants
Samples
Known GenesCCDC183, CCDC183-AS1, LCN10, LCN15, LCN6, LCN8, LOC100128593, MIR6722, SNHG7, SNORA17, SNORA43, TMEM141
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=23
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778432
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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